List of variants in gene GNPTG reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_032520.5(GNPTG):c.887G>A (p.Arg296Gln)	rs561640998	0.00010
NM_032520.4(GNPTG):c.499dup (p.Leu167Profs)	rs756959430
NM_032520.5(GNPTG):c.190_193dup (p.Phe65fs)	rs2141861740
NM_032520.5(GNPTG):c.819_822del (p.Thr274fs)	rs2548191579
NM_032520.5(GNPTG):c.823_823+1insTGCT	rs2548191594

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